Guidance

Smallpox vaccine PGD template

PGD template for administering smallpox vaccine in response to monkeypox.mpox (monkeypox).

Applies to England

Documents

Smallpox patient group direction (PGD) template

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Details

This patient group direction (PGD) template supports the administration of the smallpox vaccine, modified vaccinia virus Ankara - Bavarian Nordic (MVA-BN), to individuals identified for immunisation in response to monkeypox.mpox.

The smallpox PGD version 2.003.00 is valid from 1715 OctoberSeptember 20222023 to 1615 OctoberSeptember 2023.2024.

For information:

  • at present, there are no stocks of the UK licensed MVA-BN vaccine Imvanex® available
  • the Medicines and Healthcare products Regulatory Agency (MHRA) have granted batch-specific variation for batchesbatch FDP00012number and FDP00072 toof the US licensed vaccine Jynneos®,Jynneos® inis view of the urgencyonly ofbatch theallowed need to manage the monkeypox outbreak only vaccines from these 2 batches can be used under thethis UKHSA smallpox PGD

Practitioners must not use this PGD template until it has been authorised in Section 2. This is a legal requirement (see Human Medicines Regulations 2012). Practitioners should follow local policy or procedures to access authorised PGD documents.

This PGD template should used with reference to current national recommendation on monkeypoxmpox vaccination, the Green Book and the Direct Healthcare Professional Communication letter from Bavarian Nordic the differences between Imvanex® brand (licensed in GB/UK)UK) and Jynneos® brand (licensed in US) of live modified vaccinia virus Ankara.

Published 5 August 2022
Last updated 205 OctoberSeptember 20222023 + show all updates
  1. Added version 3 - see page 2 for change history.

  2. Added version 2.00 – details of changes on page 2 and updated batch information.

  3. Corrected review date.

  4. First published.